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E test r

Manufactured by bioMérieux
Sourced in United States, France

E-Test(r) is a quantitative antimicrobial susceptibility testing (AST) method developed by bioMérieux. It provides minimum inhibitory concentration (MIC) values for a wide range of antimicrobial agents against clinically relevant microorganisms.

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2 protocols using e test r

1

Antifungal Susceptibility Testing Protocols

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Clinical laboratories can determine susceptibility to antifungals through a series of
commercially available systems, including the Sensititre YeastOne(r) panel (TREK
Diagnostic Systems, Cleveland, USA) and the Vitek 2 system, both based on
microdilution methods, or agar-based assays, e.g. test strips (E-Test(r), bioMérieux;
MIC(r), Oxoid) and discs impregnated with a single antifungal agent.
In order to choose a commercial method, first of all, the laboratory should be aware
of the commercial techniques results considering the susceptibility of each drug to a
particular fungus, comparing the CLSI and the EUCAST reference procedures. In
general, the correlation is based on the essential agreement (EA), defined as the
discrepancies between MIC results of no more than ± 2 twofold dilutions, and the
categorical agreements (CA). The latter depends on the existence of interpretative
break points27 (link)
,48 . Of note, the laboratory should perform
tests strictly as instructed in the commercial guidelines to get reliable results.
Additionally, quality control strains, such as C. krusei ATCC 6258
and C. parapsilosis ATCC 22019 must be included in each commercial
system batch, and be ascertain that all MIC values are within the expected ranges.
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2

Characterizing Antifungal Susceptibility of Candida Strains

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Eighteen Candida strains (three strains of each of six species) were selected depending on their prevalence in medical pathologies. They were all fully characterized using MALDI-TOF MS (VITEK MS, bioMérieux, Marcy-l' Étoile, France) and their antifungal susceptibility tested (eTest R , bioMérieux) as recommended by the manufacturer, to verify expected results regarding azoles susceptibility. Four were American Type Culture Collection (ATCC, Manassas, VA, USA) strains: azole-susceptible C. albicans ATCC 90028, azolesusceptible C. albicans ATCC 10231, azole-susceptible C. glabrata ATCC MYA2950, and fluconazole-resistant C. krusei ATCC 6258). The 14 others were isolated from clinical samples: one azole susceptible C. albicans, two azole susceptible C. glabrata (fluconazole = 2 μg/ml, voriconazole = 0.023 μg/ml), three azole-resistant C. glabrata (fluconazole >256 μg/ml; voriconazole >32 μg/ml), two naturally resistant C. krusei and three of each naturally resistant C. lipolytica and C. inconspicua. 16 Before use, to work with strains in exponential growth phase, all were cultured for 24 hours on ChromID CAN2 (bioMérieux).
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